Autism Speaks, the world's leading autism science and advocacy organization, today launched the web-based portal for its MSSNG database, making the resource available to researchers worldwide. The MSSNG portal enables qualified scientists to access, study and share findings on detailed genomic information from people with autism spectrum disorder and their family members. Announced in December 2014, the MSSNG project (pronounced "missing") is a significant milestone in advancing autism research. MSSNG aims to sequence the complete genomes of 10,000 individuals affected by autism and their families by early 2016 - an unprecedented undertaking that provides the global autism research community with an open resource to answer some of the most vexing questions about the disorder. This could lead to breakthroughs in identifying the causes and subtypes of autism, as well as advancing the diagnosis and personalized treatment of the disorder.
University of Toronto
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Autism Speaks launches MSSNG portal for open-access genomics research
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Boycott Of Publishing Giant Elsevier Gathers Pace
Frustrated by what they call an exploitative business model and unreasonable prices, researchers at [University of Toronto] have joined a growing movement asking: how much must we pay for knowledge?
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New Gene Sequencing Software Could Aid in Early Detection, Treatment of Cancer
A research team from the United States and Canada has developed and successfully tested new computational software that determines whether a human DNA sample includes an epigenetic add-on linked to cancer and other adverse health conditions. In the Feb. 20 issue of the journal Nature Methods, team members from Johns Hopkins University, the Ontario Institute for Cancer Research and the University of Toronto detailed their promising new method of detecting the presence of an extra mark on DNA called cytosine methylation...
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New Open Source Gene Sequencing Software Could Aid in Early Detection, Treatment of Cancer
A research team from the United States and Canada has developed and successfully tested new computational software that determines whether a human DNA sample includes an epigenetic add-on linked to cancer and other adverse health conditions. In the Feb. 20 issue of the journal Nature Methods, team members from Johns Hopkins University, the Ontario Institute for Cancer Research and the University of Toronto detailed their promising new method of detecting the presence of an extra mark on DNA called cytosine methylation...
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The Ontario Institute for Cancer Research and the Structural Genomics Consortium develop and give away new drug-like molecule to help crowd-source cancer research.
Through a novel open source approach the molecule has been made freely available to the cancer research community to help discover new therapeutic strategies for cancer patients sooner...Researchers from the Ontario Institute for Cancer Research (OICR) and the Structural Genomics Consortium (SGC) at the MaRS Discovery District in Toronto have developed a new drug prototype called OICR-9429 and made it freely available to the research community. Already research conducted by international groups using OICR-9429 has shown it to be effective in stopping cancer cell growth in breast cancer cell lines and a specific subtype of leukemia cells.
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